Type | Description |
---|---|
Definition | dystonin |
Date | Results | Publications |
---|---|---|
2020-03-07 12:16:00 | FLG and DST support melanoma cell growth in vitro and in vivo. Growth effects of JUP were only evident in vivo, and may be mediated, in part, by enhancing angiogenesis. In addition, growth-promoting effects of FLG and DST in vitro suggest that these genes may also support melanoma cell proliferation through angiogenesis-independent pathways. | 31425296 |
2020-01-18 11:52:00 | Our finding suggests that DST alteration may involve in the mechanism of diabetic dementia | 30963337 |
2019-05-25 10:59:00 | Microtubule instability is not central to initiation of dystonia musculorum (Dstdt) pathogenesis, though it may contribute to disease severity. Maintenance of microtubule stability in Dstdt-Tg4 dorsal root ganglia could be attributed to an upregulation in Dst-A3 expression as a compensation for the absence of Dst-A1 and -A2 in Dstdt-Tg4 sensory neurons. | 29982604 |
2018-02-10 11:45:00 | The present study identified novel mutant mice with a mild dt phenotype of sensory neurodegeneration and movement disorder. | 27693510 |
2016-08-06 11:08:00 | oligodendrocytes do not have an intrinsic requirement for neuronal dystonin for differentiation and myelination. | 26886550 |
Type | IDs |
---|---|
Synonymous | 2310001O04Rik, A830042E19Rik, AW554249, BP230, BPAG1-n, Bpag, Bpag1, Macf2, ah, athetoid, dt, mKIAA0728, nmf203, nmf339 |
Gene |
UniProtKB-ID:
DYST_MOUSE,
S4R1P5_MOUSE
UniprotKB:
Q91ZU6,
S4R1P5
UniParc:
UPI0000DBD9C1,
UPI0004AC3F5F,
UPI0002B83574,
UPI0004AC3F65,
UPI0000DBD9C2,
UPI00005C8BBC,
UPI0000D67AFE,
UPI0002B83576
EMBL:
AF396877,
AF396878,
AK037206,
U22452,
U25158,
AC123072,
AF396879,
AC124386,
DQ023311,
AF115383,
AB085694,
AK051626,
AC127433,
DQ463750
Ensembl:
ENSMUSG00000026131
KO:
mmu:13518
|
Nucleutide sequences |
EMBL-CDS:
AAY46942.1,
AAK83383.1,
AAC52231.1,
AAD22959.1,
BAC34695.1,
AAC52230.1,
BAC29753.1,
AAK83384.1,
AAK83382.1,
ABF00406.1,
BAB93448.1
Ensembl_TRS:
ENSMUST00000183302,
ENSMUST00000097786,
ENSMUST00000097785,
ENSMUST00000183034
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000138376,
ENSMUSP00000095392,
ENSMUSP00000095393,
ENSMUSP00000138308
RefSeq:
XP_017170205.1,
XP_030102360.1,
XP_017170239.1,
NP_001263693.1,
NP_034211.2,
XP_017170140.1,
XP_017170176.1,
XP_006495748.1,
XP_017170337.1,
XP_006495749.1,
XP_006495743.1,
XP_017170211.1,
XP_017170110.1,
XP_006495747.1,
NP_598594.2,
XP_036014401.1,
XP_006495742.1,
XP_006495737.1,
XP_036014447.1,
XP_017170300.1,
XP_006495753.1,
XP_017170195.1,
XP_017170178.1,
XP_017170230.1,
XP_017170201.1,
XP_017170154.1,
XP_017170165.1,
XP_017170283.1,
XP_017170357.1,
XP_006495745.1,
XP_017170124.1,
NP_604443.2,
XP_006495729.1,
XP_006495741.1,
XP_030102561.1,
XP_006495754.1,
XP_006495732.1,
XP_006495751.1
|
Others |
UniRef100:
UniRef100_Q91ZU6,
UniRef100_S4R1P5
UniRef90:
UniRef90_S4R1P5,
UniRef90_Q91ZU6
UniRef50:
UniRef50_Q91ZU6,
UniRef50_Q03001
UniGene:
Mm.336625,
Mm.478284,
Mm.487428
CCDS:
CCDS35534.1,
CCDS35535.1,
CCDS69875.1
|
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Refseq |
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